About this trial
Tobacco use is the leading cause of preventable death in the U.S., with 480,000 deaths per year and 7.7 million deaths globally. A major clinical symptom associated with abstinence from both licit and illicit drugs is insomnia, which is a clinically verified, major risk factor for relapse. Roughly half of the 40 million smokers in the U.S. attempt to quit annually, with very low rates of success. One major hurdle is poor sleep quality during abstinence. Compounding the problem is that some pharmaceuticals to help reduce smoking can increase insomnia. Poor sleep is recognized as a major impediment to maintaining abstinence from several drugs of abuse, including nicotine. Blockers of orexin have recently been proposed as a promising therapy for smoking cessation. Insomnia has been reported in up to 40% of smokers, and 80% report regular sleep disturbances, which can be amplified during abstinence. A new orexin blocker, daridorexant, was FDA approved within the past two years for the treatment of insomnia, and while it has been tested in healthy individuals with insomnia, it has not been tested in smokers, who suffer from insomnia, particularly during the withdrawal phase when trying to quit. Daridorexant has an improved profile of beneficial effects for those with insomnia, the most notable advantage being its shorter duration of action that promotes daytime alertness, which is problematic for both active smokers and smokers during withdrawal. Poor sleep leads to daytime sleepiness, which often leads to smoking to maintain alertness.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult participants who are cigarette smokers, 18-55 years of age.
Smokers: greater than 10 cigarettes/day.
Smoking for 1 year or longer.
Willingness to try to reduce or stay abstinent from cigarettes, smoking cessation aides (including nicotine gum or patches), smokeless tobacco, or electronic cigarettes for 3 weeks during the study.
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Daridorexant 50 mg
DrugActive daridorexant vs placebo comparator in smokers with insomnia
Placebo
Other interventionPlacebo in Smokers
Treatment groups
Trial outcomes
Primary outcomes
Sleep Quality
Sleep device to assess: latency to sleep, number of awakenings during the night, and sleep stages.
Daytime alertness
Assess daytime alertness using a 5 min psychomotor vigilance task. Higher score indicates lower alertness.
Insomnia Severity Index
Assesses extent of insomnia. Range is 0-28. Higher score indicates high level of insomnia.
Sleep Quality-sleep diary
Daily sleep diary to assess self-reported sleep
Secondary outcomes
Fagerstrom
Assesses extent of nicotine dependence. Range is 0-10. Higher score indicates higher dependence.
Smoking History and Habits
Must smoke 10 or more cigarettes per day.
Minnesota Scale Withdrawal from Nicotine
Assesses nicotine withdrawal symptoms over last 24 hr. Range is 0-60, higher score indicating higher withdrawal signs/symptoms.
QSU Brief Smoking Desire
Assesses desire to smoke. Range 7-49. Higher score indicates higher craving to smoke.
Other outcomes
Morningness/Eveningness questionnaire
Scores range from 16-83, with higher score indicating morning type and lower score evening type.
GAD-67 Anxiety
Assesses anxiety levels over last 2 weeks. Range is 0-21, higher score indicating higher anxiety.
Patient Health Questionnaire 9 (PHQ 9 Depression)
Assesses depression levels. Range is 1-27, higher score indicating higher depression.
Readiness to Quit
Readiness to quit tobacco. Scale is 1-10, with higher score indicating more important to quit.
Sponsors and contacts
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Legacy Health System
Lead sponsor
Washington State University
Collaborator
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